| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93467395-93467546 | Common:1; Rare:50 | ||||
| chr12:93571728-93571902 | Common:6; Rare:66 | ||||
| chr12:93572475-93572831 | Common:1; Rare:98 | ||||
| chr12:93677262-93677399 | Rare:29 | ||||
| chr12:94459802-94460064 | Common:3; Rare:76 | ||||
| chr12:95003605-95003835 | Common:3; Rare:97; Clinvar (benign):6 | ||||
| chr12:95073398-95073680 | Common:2; Rare:93 | ||||
| chr12:95217360-95217886 | Common:6; Rare:142 | ||||
| chr12:95218160-95218318 | Common:2; Rare:38 | ||||
| chr12:95473851-95474016 | Common:1; Rare:49 | ||||
| chr12:95474020-95474344 | Common:2; Rare:134 | ||||
| chr12:95484561-95484856 | Common:2; Rare:56 | ||||
| chr12:95548789-95548974 | Common:4; Rare:59 | ||||
| chr12:95551414-95551619 | Common:2; Rare:39 | ||||
| chr12:95858804-95859173 | Common:3; Rare:114 |